The Editorial Executive Committee welcomes letters, which should be less than 250 words. Before a decision to publish is made, letters which refer to a published article may be sent to the author for a response. Any letter may be sent to an expert for comment. When letters are published, they are usually accompanied in the same issue by their responses or comments. The Committee screens out discourteous, inaccurate or libellous statements. The letters are sub-edited before publication. Authors are required to declare any conflicts of interest. The Committee's decision on publication is final.
Letter to the Editor
Editor, – The New drug comment about balsalazide sodium (Aust Prescr 2005;28:104-6) described the use of this product by citing two 1998 studies which compared it to mesalazine in double-blind trials with ulcerative colitis patients.12
I wish to bring to your attention that the conclusions of these studies are not generalisable to the mesalazine products available in Australia, since the mesalazine product used in these studies (Asacol) is not marketed in this country. Asacol has a different coating from the mesalazine products marketed in Australia.
There are several mesalazine formulations available globally, which have different coatings and therefore different release mechanisms345 which may lead to different therapeutic efficacy. These different formulations are also supplied in different strengths. The only two oral formulations of mesalazine available in Australia are Salofalk and Mesasal which are delayed-release preparations of mesalazine coated with a resin that dissolves at a pH greater than six (the approximate pH of the ileum/colon). In contrast, Asacol consists of 400 mg of mesalazine destined for release in the terminal ileum or colon as its resin coating dissolves at a pH greater than seven.
Mesalazine products with different coatings are not therapeutically equivalent and are not interchangeable. The results of the Abacus Investigator Group studies therefore cannot be generalised to all mesalazine preparations, including the oral preparations available in Australia. Such generalisations would be misleading.
The comment also claims that 'mesalazine is absorbed, but is rapidly metabolised and excreted in the urine'. However, like balsalazide, very little mesalazine is systemically absorbed after being orally administered. The active drug is believed to act topically on the intestine and the main route of elimination is the faeces.6
Medical Affairs Associate
Orphan Australia Pty Ltd
- Abacus Investigator Group. Balsalazide is more effective and better tolerated than mesalamine in the treatment of acute ulcerative colitis. Gastroenterology 1998;114:15-22.
- Abacus Investigator Group. Maintenance of remission of ulcerative colitis: a comparison between balsalazide 3 g daily and mesalazine 1.2 g daily over 12 months. Aliment Pharmacol Ther 1998;12:1207-16.
- Tromm A, Griga T, May B. Oral mesalazine for the treatment of Crohn's disease: clinical efficacy with respect to pharmacokinetic properties. Hepato-Gastroenterology 1999;46:3124-35.
- Sutherland L, MacDonald JK. Oral 5-aminosalicylic acid for induction of remission in ulcerative colitis. The Cochrane Database of Systematic Reviews 2003, Issue 3. Art. No: CD000543 DOI: 10.1002/14651858. CD000543.
- Sutherland L, Roth D, Beck P, May G, Makiyama K. Oral 5-aminosalicylic acid for maintenance of remission in ulcerative colitis. The Cochrane Database of Systematic Reviews 2002, Issue 4. Art. No: CD000544. DOI 10.1002/14651858 CD000544.
- Orphan. Salofalk tablets and granules. Product information.